| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 6 | g.157181168G>T | CA366228517 | ARID1B | c.3545G>T (p.Gly1182Val) c.3614G>T (p.Gly1205Val) c.3833G>T (p.Gly1278Val) c.1718G>T (p.Gly573Val) c.3584G>T (p.Gly1195Val) c.3296G>T (p.Gly1099Val) c.1862G>T (p.Gly621Val) c.1025G>T (p.Gly342Val) c.659G>T (p.Gly220Val) c.3704G>T (p.Gly1235Val) n.1701G>T c.1072G>T c.986G>T n.370G>T c.1046G>T (p.Gly349Val) c.1205G>T (p.Gly402Val) c.3335G>T (p.Gly1112Val) c.1721G>T (p.Gly574Val) c.497G>T (p.Gly166Val) c.906G>T c.3455G>T (p.Gly1152Val) c.2534G>T (p.Gly845Val) c.2354G>T (p.Gly785Val) c.2114G>T (p.Gly705Val) c.1733G>T (p.Gly578Val) c.596G>T (p.Gly199Val) c.3665G>T (p.Gly1222Val) c.3566G>T (p.Gly1189Val) c.3536G>T (p.Gly1179Val) c.3506G>T (p.Gly1169Val) c.3377G>T (p.Gly1126Val) c.3356G>T (p.Gly1119Val) n.3748G>T | dbSNP |
| 6 | g.157181168G>C | CA366228512 | ARID1B | c.3545G>C (p.Gly1182Ala) c.3614G>C (p.Gly1205Ala) c.3833G>C (p.Gly1278Ala) c.1718G>C (p.Gly573Ala) c.3584G>C (p.Gly1195Ala) c.3296G>C (p.Gly1099Ala) c.1862G>C (p.Gly621Ala) c.1025G>C (p.Gly342Ala) c.659G>C (p.Gly220Ala) c.3704G>C (p.Gly1235Ala) n.1701G>C c.1072G>C c.986G>C n.370G>C c.1046G>C (p.Gly349Ala) c.1205G>C (p.Gly402Ala) c.3335G>C (p.Gly1112Ala) c.1721G>C (p.Gly574Ala) c.497G>C (p.Gly166Ala) c.906G>C c.3455G>C (p.Gly1152Ala) c.2534G>C (p.Gly845Ala) c.2354G>C (p.Gly785Ala) c.2114G>C (p.Gly705Ala) c.1733G>C (p.Gly578Ala) c.596G>C (p.Gly199Ala) c.3665G>C (p.Gly1222Ala) c.3566G>C (p.Gly1189Ala) c.3536G>C (p.Gly1179Ala) c.3506G>C (p.Gly1169Ala) c.3377G>C (p.Gly1126Ala) c.3356G>C (p.Gly1119Ala) n.3748G>C | ClinVar dbSNP |
| 6 | g.157181168G>A | CA248922 | ARID1B | c.3545G>A (p.Gly1182Asp) c.3614G>A (p.Gly1205Asp) c.3833G>A (p.Gly1278Asp) c.1718G>A (p.Gly573Asp) c.3584G>A (p.Gly1195Asp) c.3296G>A (p.Gly1099Asp) c.1862G>A (p.Gly621Asp) c.1025G>A (p.Gly342Asp) c.659G>A (p.Gly220Asp) c.3704G>A (p.Gly1235Asp) n.1701G>A c.1072G>A c.986G>A n.370G>A c.1046G>A (p.Gly349Asp) c.1205G>A (p.Gly402Asp) c.3335G>A (p.Gly1112Asp) c.1721G>A (p.Gly574Asp) c.497G>A (p.Gly166Asp) c.906G>A c.3455G>A (p.Gly1152Asp) c.2534G>A (p.Gly845Asp) c.2354G>A (p.Gly785Asp) c.2114G>A (p.Gly705Asp) c.1733G>A (p.Gly578Asp) c.596G>A (p.Gly199Asp) c.3665G>A (p.Gly1222Asp) c.3566G>A (p.Gly1189Asp) c.3536G>A (p.Gly1179Asp) c.3506G>A (p.Gly1169Asp) c.3377G>A (p.Gly1126Asp) c.3356G>A (p.Gly1119Asp) n.3748G>A | ClinVar dbSNP COSMIC COSMIC |
| 6 | g.157181168G= | CA1675534293 | ARID1B | c.3545G= (p.Gly1182=) c.3614G= (p.Gly1205=) c.3833G= (p.Gly1278=) c.1718G= (p.Gly573=) c.3584G= (p.Gly1195=) c.3296G= (p.Gly1099=) c.1862G= (p.Gly621=) c.1025G= (p.Gly342=) c.659G= (p.Gly220=) c.3704G= (p.Gly1235=) n.1701G= c.1072G= c.986G= n.370G= c.1046G= (p.Gly349=) c.1205G= (p.Gly402=) c.3335G= (p.Gly1112=) c.1721G= (p.Gly574=) c.497G= (p.Gly166=) c.906G= c.3455G= (p.Gly1152=) c.2534G= (p.Gly845=) c.2354G= (p.Gly785=) c.2114G= (p.Gly705=) c.1733G= (p.Gly578=) c.596G= (p.Gly199=) c.3665G= (p.Gly1222=) c.3566G= (p.Gly1189=) c.3536G= (p.Gly1179=) c.3506G= (p.Gly1169=) c.3377G= (p.Gly1126=) c.3356G= (p.Gly1119=) n.3748G= | dbSNP |